Literature DB >> 7844651

How much should I say to whom?

M I Fitch1.   

Abstract

During the past several decades, attitudes in North America have shifted with regards to disclosing information to patients about their own diagnosis. There is still debate, however, about the extent of the information that should be shared regarding treatment and prognosis. Families have their own set of needs in the face of coping with life-threatening illness and supporting the patient. Receiving clear honest information about the patient's condition, prognosis, and comfort are important to family caregivers. Resolving the issue of disclosing patient information to families demands that health care professionals engage in sensitive communication and achieve a delicate balance between the patient's right to confidentiality and meeting the family members' needs for information.

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Year:  1994        PMID: 7844651

Source DB:  PubMed          Journal:  J Palliat Care        ISSN: 0825-8597            Impact factor:   2.250


  4 in total

1.  Challenges of participatory research: reflections on a study with breast cancer self-help groups.

Authors:  Ross E. Gray; Margaret Fitch; Christine Davis; Catherine Phillips
Journal:  Health Expect       Date:  2000-12       Impact factor: 3.377

2.  The right to information for the terminally ill patient.

Authors:  E Osuna; M D Pérez-Cárceles; M A Esteban; A Luna
Journal:  J Med Ethics       Date:  1998-04       Impact factor: 2.903

3.  [Breaking of bad news. Practical advice to physicians for successful communication with patients].

Authors:  M Weber; A Werner; C Nehring; F J Tentrup
Journal:  Med Klin (Munich)       Date:  1999-08-15

4.  Development of a Question Prompt Sheet for Cancer Patients Receiving Outpatient Palliative Care.

Authors:  Joseph Arthur; Sriram Yennurajalingam; Janet Williams; Kimberson Tanco; Diane Liu; Saneese Stephen; Eduardo Bruera
Journal:  J Palliat Med       Date:  2016-05-13       Impact factor: 2.947

  4 in total

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